Neuroscience(神经科学)

Neuroscience
Neurons communicate with each other, effector organs and sensory organs through the neurotransmitter – receptor pathway at synapses. Neurotransmitters can be divided into 4 major groups: 1. Amino acids (glumate, aspartate, serine, glycine and GABA); 2. Monoamines (norepinephrine, epinephrine, dopamine, histamine, and serotonin); 3. Peptides (opioid peptides, substance P, somatostatin); and 4. Others (acetylcholine, NO, nucleosides). read more
Products for Neuroscience
- 5-HT Receptor(420)
- AChR(53)
- AChE(100)
- Alzheimer(107)
- Amyloid β(118)
- BACE(4)
- CGRP (33)
- COX(294)
- DAPK(7)
- Dopamine Receptor(290)
- GABA Receptor(155)
- Gap Junction(16)
- GluR(116)
- Histamine(2)
- Histamine Receptor(236)
- mPEGS-1(4)
- Muscarinic Receptor(41)
- Neuroscience Peptides(38)
- Nicotinic Receptor(62)
- P2 Receptor(2)
- P2X7 receptor(3)
- SSRIs(5)
- Substance P/NK1 Receptor(20)
- NMDA(2)
- Beta-secretase(25)
- CaMK(32)
- Dopamine Transporter(20)
- Monoamine Oxidase(91)
- Serotonin Transporter(57)
- nAChR(100)
- iGluR(155)
- Neurokinin Receptor(75)
- MCHR1 (GPR24)(16)
- mAChR(183)
- GPR139(4)
- Cholecystokinin Receptor(25)
- Behavioral Neuroscience(353)
- DREADD(1)
- Huntington(14)
- Neuroendocrinology(64)
- Neuroprotection(117)
- Ophthalmology(158)
- Pain Research(229)
- Parkinson(73)
- Prion(7)
- Seizure Disorders(94)
- Cholinesterases(13)
- Tau Protein(4)
- Neurodegenerative Disorders(5)
- Cholinesterase (ChE)(3)
- Amyloid-β(9)
- γ-secretase(1)
- Ischemia(3)
- Cat.No. 产品名称 Information
-
GC18118
SDZ 220-581
(S)-ALPHA-氨基-2'-氯-5-(膦酰基甲基)-[1,1'-联苯]-3-丙酸,SDZ 220 581
SDZ 220-581 是一种具有口服活性、强效、竞争性 NMDA 受体拮抗剂,pKi 值为 7.7。 -
GC10107
SB-222200
3-甲基-2-苯基-N-((1S)-1-苯基丙基)喹啉-4-甲酰胺,SB 222200;SB222200
An NK3 receptor antagonist -
GC13016
Safinamide
沙芬酰胺; FCE 26743; EMD 1195686
Safinamide 是一种强效、选择性和可逆的单胺氧化酶 B (MAO-B) 抑制剂 (IC50=0.098 μM),优于 MAO-A (IC50=580 μM)。 -
GC11729
RS 127445
2-氨基-4-(4-氟萘-1-基)-6-异丙基嘧啶,RS-127445; MT 500; RS127445
A 5-HT2B receptor antagonist -
GC16017
Rotigotine hydrochloride
罗替戈汀盐酸盐; N-0923 Hydrochloride
A non-selective dopamine receptor agonist -
GC10614
Rotigotine
罗替戈汀; N-0437; N-0923
A non-selective dopamine receptor agonist -
GC12102
RJR-2403 oxalate
(3E)-N-甲基-4-(3-吡啶基)-3-丁烯-1-胺草酸盐,(E)-Metanicotine oxalate; Rivanicline oxalate; RJR 2403 oxalate
RJR-2403 oxalate (RJR-2403 oxalate; (E)-Metanicotine oxalate) 是一种神经元烟碱受体激动剂,对 α4β2 亚型 (Ki=26 nM) 具有高选择性; > 1,000 倍的选择性比 α7 受体(Ki = 3.6 μM)。 -
GC10267
Rivastigmine
卡巴拉汀; S-Rivastigmine
A cholinesterase inhibitor -
GC12599
Retigabine dihydrochloride
瑞替加滨,D 20443 dihydrochloride;D-20443 dihydrochloride;D20443 dihydrochloride
An Analytical Reference Standard -
GC14167
Quetiapine
喹硫平; ICI204636
Quetiapine是一种5-HT受体激动剂,对人类5-HT1A受体的 pEC50为4.77。Quetiapine是一种多巴胺受体拮抗剂,对人类D2受体的pIC50为6.33。Quetiapine是一种非典型抗精神病药,用于治疗精神分裂症、躁郁症和重度抑郁症。 -
GC13625
Pramipexole dihydrochloride
盐酸普拉克索
A dopamine D2S, D2L, D3, and D4 receptor agonist -
GC11382
Pitolisant hydrochloride
1-[3-[3-(4-氯丙基)丙氧基]丙基]-哌啶盐酸盐,Ciproxidine;BF 2649;BF2649;BF-2649
A histamine H3 receptor antagonist and inverse agonist -
GC14849
Paradol
姜酮酚; [6]-Gingerone; [6]-Paradol
A phenolic ketone with diverse biological activities -
GC17233
Olcegepant
N-[2-[5-氨基-1(S)-[4-(4-吡啶基)哌嗪-1-甲酰基]戊基氨基]-1(R)-(3,5-二溴-4-羟基苄基)-2-氧代乙基]-4-(2-氧代-1,2,3,4-四氢喹唑啉-3-基)哌啶-1-甲酰胺,BIBN-4096; BIBN-4096BS;BIBN4096BS; BIBN 4096BS
Olcegepant (BIBN-4096) 是一种有效的、选择性的降钙素基因相关肽 1 (CGRP1) 受体的非肽拮抗剂,对人 CGRP 的 IC50 为 0.03 nM 和 Ki 为 14.4 pM。 -
GC10270
Noopept
N-(1-(苯基乙酰基)-L-脯氨酰)甘氨酸乙酯,GVS-111;GVS111;GVS 111;SGS-111;SGS 111;SGS111
An Analytical Reference Standard -
GC11097
MPTP hydrochloride
1-甲基-4-苯基-1,2,3,6-四氢吡啶盐酸盐,MPTP
MPTP(1-甲基-4-苯基-1,2,3,6-四氢吡啶)是一种神经毒性物质,它是MPP+的前体,对多巴胺能神经元有毒,并导致帕金森病。 -
GC16365
MK-3207
(8R)-8-(3,5-二氟苯基)-10-氧代-N-[(2R)-1,1',2',3-四氢-2'-氧代螺[2H-茚-2,3'-[3H]吡咯并[2,3-B]吡啶]-5-基]-6,9-二氮杂螺[4.5]癸烷-9-乙酰胺,MK3207;MK 3207
MK-3207 是一种具有口服活性、高度选择性和物种特异性的 CGRP 受体拮抗剂(对于人 CGRP 受体:IC50=0.12 nM;Ki=0.024 nM)。 -
GC16478
MK-0974
N-[(3R,6S)-6-(2,3-二氟苯基)六氢-2-氧代-1-(2,2,2-三氟乙基)-1H-氮杂卓-3-基]-4-(2,3-二氢-2-氧代-1H-咪唑并[4,5-B]吡啶-1-基)-1-哌啶甲酰胺,Telcagepant;MK0974;MK 0974
A CGRP receptor antagonist -
GC11743
MF63
2-(9-氯-1H-菲并[9,10-D]咪唑-2-基)-1,3-苯二甲腈,MF 63; MF-63
A potent, selective, and orally active mPGES-1 inhibitor -
GC16249
Metoclopramide
胃复安
Metoclopramide(胃复安)是一种有效的5-HT3和多巴胺D2受体拮抗剂,IC50 值分别为308nM和483nM。 -
GC13024
Metiamide
甲硫米特,SK&F 92058
Metiamide (SK&F 92058) 是一种组胺 H2 受体拮抗剂,由另一种 H2 拮抗剂布立马胺发展而来。 -
GC17039
LY 344864
LY344864;LY-344864
A 5-HT1F receptor antagonist -
GC15998
LX-1031
4-[2-氨基-6-[(1R)-2,2,2-三氟-1-(3'-甲氧基联苯-4-基)乙氧基]嘧啶-4-基]-L-苯丙氨酸,LX1031; LX 1031
LX-1031 是一种有效的、可口服的色氨酸 5-羟化酶 (TPH) 抑制剂,可减少外周血清素 (5-HT) 的合成。 -
GC11962
Lu AE58054 Hydrochloride
N-[2-(6-氟-1H-吲哚-3-基)乙基]-3-(2,2,3,3-四氟丙氧基)苄基胺单盐酸盐,Lu AE 58054 Hydrochloride
A 5-HT6 receptor antagonist -
GC14252
(-)-Stepholidine
左旋千金藤啶碱,Stepholidine;(-)-Stepholidine;L-SPD
A dopamine receptor antagonist and 5-HT1A partial agonist -
GC10629
KN-93
N-[2-[N-(4-氯肉桂)-N-甲基氨基]苯基]-N-(2-羟乙基)-4-甲氧苯磺酰胺磷酸酯盐,KN 93;KN93
Selective inhibitor of Ca2+/calmodulin-dependent kinase type II -
GC16981
KN-92 phosphate
KN-92磷酸盐,KN 92 phosphate;KN92 phosphate
KN-92 phosphate 是 KN-93 的无活性衍生物,没有 CaM 激酶抑制活性。 KN-92 磷酸盐旨在用作旨在阐明 KN-93 拮抗剂活性的研究中的对照化合物。 KN-93 是一种细胞渗透性、可逆性和竞争性 CaMKII 抑制剂。 -
GC15988
KN-92 hydrochloride
KN-92盐酸盐,KN 92 hydrochloride;KN92 hydrochloride
An inactive control compound for a CaMKII inhibitor -
GC14132
KN-92
KN 92;KN92
An inactive control compound for a CaMKII inhibitor -
GC17419
Iguratimod
艾拉莫德; T614
A DMARD and COX-2 inhibitor -
GC17657
Hoechst 34580
HOE 34580;Proamine;Hoechst-34580;Hoechst34580
The nucleic acid stain Hoechst 34580 (Ex/Em: 392/440 nm) is frequently utilized as a cell-permeable nuclear counterstain that emits a blue fluorescence upon binding to dsDNA.
-
GC12398
Granisetron
格拉司琼; BRL 43694
Granisetron (BRL 43694) 是一种血清素 5-HT3 受体拮抗剂,用作止吐剂,用于治疗化疗后的恶心和呕吐。 -
GC16573
Galanthamine
加兰他敏; Galantamine
An alkaloid with AChE inhibitory and nAChR potentiating activities -
GC11768
FK 3311
N-[4-乙酰基-2-(2,4-二氟苯氧基)苯基]-甲烷磺酰胺,FK-3311;FK3311
A COX-2 inhibitor -
GC11091
EVP-6124 hydrochloride
(R)-7-氯-N-(奎宁环-3-基)苯并[B]噻吩-2-甲酰胺盐酸盐,EVP 6124 hydrochloride;EVP6124 hydrochloride
A partial agonist of α7 subunit-containing nAChRs -
GC15941
EVP-6124
EVP 6124;EVP6124
A partial agonist of α7 subunit-containing nAChRs -
GC10429
Etoricoxib
依托考昔; MK-0663; L-791456
A selective COX-2 inhibitor -
GC15264
Etifoxine hydrochloride
盐酸艾替伏辛,Stresam;HOE 36-801
A positive allosteric modulator of GABAA receptors -
GC16089
Ebrotidine
乙溴替丁,FI 3542;Ulsanic;FI-3542;FI3542
Ebrotidine(FI 3542) 是一种竞争性 H2 受体拮抗剂 (Ki= 127.5 nM),具有有效的抗分泌活性和明显的胃保护作用。 -
GC16073
Dronedarone
决奈达隆; SR 33589
An antiarrhythmic agent -
GC12782
CP-809101 hydrochloride
2-[(3-氯苯基)甲氧基]-6-(1-哌嗪基)吡嗪盐酸盐,CP809101 hydrochloride;CP 809101 hydrochloride
A potent 5-HT2C receptor agonist -
GC17183
CP-809101
6'-(3-氯苄基氧基)-3,4,5,6-四氢-2H-[1,2']联吡嗪,CP809101;CP 809101
A potent 5-HT2C receptor agonist -
GC10822
Clozapine N-oxide (CNO)
氯氮平N-氧化物
Clozapine N-oxide(CNO)是一种强效的多巴胺拮抗剂,也是一种选择性肌动蛋白M4受体(EC50=11 nM)激动剂。 -
GC17701
Clemizole hydrochloride
盐酸克立咪唑
An antihistamine and TRPC5 channel blocker -
GC12444
Clemizole
吡咯咪唑
An antihistamine and TRPC5 channel blocker -
GC17157
Cevimeline hydrochloride hemihydrate
盐酸西维美林半水合物; SNI-2011; AF102B hydrochloride hemihydrate
Cevimeline hydrochloride hemihydrate (SNI-2011) 是乙酰胆碱的奎宁环衍生物,是一种选择性和口服活性的毒蕈碱 M1 和 M3 受体激动剂。 -
GC14215
Cevimeline
西维美林; AF102B
A muscarinic receptor agonist -
GC10185
Cetirizine
西替利嗪
西替利嗪是一种第二代抗组胺药,是羟嗪的羧化代谢物,是一种特异性的、具有口服活性的长效组胺 H1 受体拮抗剂。 -
GC15985
Cariprazine
卡利拉嗪; RGH-188
An atypical antipsychotic -
GC13705
BMS-927711
瑞美吉泮,BMS 927711;BMS927711
A CGRP receptor antagonist